The IFITM5 mutation c.-14C > T results in an elongated transcript expressed in human bone; and causes varying phenotypic severity of osteogenesis imperfecta type V

Overview of attention for article published in BMC Musculoskeletal Disorders, March 2014

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Background: The genetic mutation resulting in osteogenesis imperfecta (OI) type V was recently characterised as a... http://t.co/h5Tph6tL9g

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